← Back to catalogue
Adapters for lenses and endoscopes
EUDAMEDFDA UDIClass I (EU MDR)
Ref 8580.91Model 10000201206
Identity
- Trade Name
- NA FDA UDI
- Generic Name
- Endoscope camera adaptor FDA UDI
- Device Name
- Adapters for lenses and endoscopes EUDAMEDSTERILE ADAPTER Plug-eyepiece for endoscope exchange under sterile conditions, lock mechanism FDA UDI
- Model / Reference
- 10000201206 EUDAMED8580.91 EUDAMED858091 FDA UDI
- Description
- STERILE ADAPTER Plug-eyepiece for endoscope exchange under sterile conditions, lock mechanism FDA UDI
Identifiers
- Catalog Number
- 8580.91 FDA UDI
- Primary DI / UDI-DI
- 04055207010679 EUDAMEDFDA UDI
- Basic UDI-DI
- 405520727052019-0017958QF EUDAMED
- Direct Marketing DI
- 04055207010679 EUDAMED
- FDA Product Code
- FEM FDA UDI
- EMDN Code
- Z12020480 INSTRUMENTS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Endoscope camera adaptor FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 40 Millimeter FDA UDI
Adapters for lenses and endoscopes by Richard Wolf GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 405520727052019-0017958QF | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Richard Wolf GmbH
- EUDAMED SRN
- DE-MF-000007048
Sources (2)
- EUDAMED 00cbf6fa-39d5-42a2-8e40-cee6b6d5de70 61 fields · synced Aug 4, 2026
- FDA UDI d5b5d28b-2cc5-4ad5-9613-7f8e5f4a57a6 37 fields · synced May 29, 2026